Clark Brett, Chaumel Júlia, Johanson Zerina, Underwood Charlie, Smith Moya M, Dean Mason N
Image and Analysis Centre, Core Research Labs, London, United Kingdom.
Department of Biomaterials, Max Planck Institute of Colloids and Interfaces, Potsdam, Germany.
Front Cell Dev Biol. 2022 Oct 12;10:932341. doi: 10.3389/fcell.2022.932341. eCollection 2022.
Crushing and eating hard prey (durophagy) is mechanically demanding. The cartilage jaws of durophagous stingrays are known to be reinforced relative to non-durophagous relatives, with a thickened external cortex of mineralized blocks (tesserae), reinforcing struts inside the jaw (trabeculae), and pavement-like dentition. These strategies for skeletal strengthening against durophagy, however, are largely understood only from myliobatiform stingrays, although a hard prey diet has evolved multiple times in batoid fishes (rays, skates, guitarfishes). We perform a quantitative analysis of micro-CT data, describing jaw strengthening mechanisms in (Bowmouth Guitarfish) and (White-spotted Wedgefish), durophagous members of the Rhinopristiformes, the sister taxon to Myliobatiformes. Both species possess trabeculae, more numerous and densely packed in , albeit simpler structurally than those in stingrays like and . and exhibit impressively thickened jaw cortices, often involving >10 tesseral layers, most pronounced in regions where dentition is thickest, particularly in . Age series of both species illustrate that tesserae increase in size during growth, with enlarged and irregular tesserae associated with the jaws' oral surface in larger (older) individuals of both species, perhaps a feature of ageing. Unlike the flattened teeth of durophagous myliobatiform stingrays, both rhinopristiform species have oddly undulating dentitions, comprised of pebble-like teeth interlocked to form compound "meta-teeth" (large spheroidal structures involving multiple teeth). This is particularly striking in , where the upper/lower occlusal surfaces are mirrored undulations, fitting together like rounded woodworking finger-joints. Trabeculae were previously thought to have arisen twice independently in Batoidea; our results show they are more widespread among batoid groups than previously appreciated, albeit apparently absent in the phylogenetically basal Rajiformes. Comparisons with several other durophagous and non-durophagous species illustrate that batoid skeletal reinforcement architectures are modular: trabeculae can be variously oriented and are dominant in some species (e.g. , ), whereas cortical thickening is more significant in others (e.g. ), or both reinforcing features can be lacking (e.g. , ). We discuss interactions and implications of character states, framing a classification scheme for exploring cartilage structure evolution in the cartilaginous fishes.
压碎并吞食硬壳猎物(食硬食性)对身体机能要求很高。已知食硬食性的黄貂鱼的软骨颚相对于非食硬食性的近亲有所强化,其矿化块(嵌片)的外部皮质增厚,颚内有加固支柱(小梁),还有类似铺路石的齿列。然而,尽管硬壳猎物饮食习性在鲼形目鱼类(黄貂鱼、鳐、犁头鳐)中已多次进化,但目前对于这些针对食硬食性的骨骼强化策略的了解,很大程度上仅来自鲼形目黄貂鱼。我们对显微CT数据进行了定量分析,描述了犁头鳐目(鲼形目的姐妹分类群)中食硬食性成员弯口犁头鳐和白点楔吻鲟的颚强化机制。这两个物种都有小梁,在弯口犁头鳐中数量更多且排列密集,尽管其结构比像斑鳐和黄貂鱼这样的黄貂鱼的小梁更简单。弯口犁头鳐和白点楔吻鲟的颚皮质显著增厚,通常涉及超过10层嵌片,在齿列最厚的区域最为明显,尤其是在弯口犁头鳐中。这两个物种的年龄序列表明,嵌片在生长过程中会变大,在两个物种较大(年龄较大)个体的颚口表面,嵌片会增大且形状不规则,这可能是衰老的一个特征。与食硬食性的鲼形目黄貂鱼扁平的牙齿不同,犁头鳐目这两个物种都有奇特的波浪状齿列,由卵石状牙齿相互嵌合形成复合“超齿”(由多颗牙齿组成的大型球状结构)。这在弯口犁头鳐中尤为显著,其上/下咬合面呈镜像波浪状,像圆形木工指接一样相互契合。小梁以前被认为在鲼形目中独立出现过两次;我们的研究结果表明,它们在鲼形目群体中的分布比以前认为的更广泛,尽管在系统发育上处于基部的鳐形目中显然不存在。与其他几种食硬食性和非食硬食性物种的比较表明,鲼形目骨骼强化结构是模块化的:小梁可以有不同的方向,在一些物种(如弯口犁头鳐、白点楔吻鲟)中占主导地位,而在其他物种(如斑鳐)中皮质增厚更为显著,或者两种强化特征都可能不存在(如某些鳐类)。我们讨论了性状状态的相互作用和影响,构建了一个分类方案,用于探索软骨鱼类软骨结构的进化。